NCT07080151

Brief Summary

The purpose of this registry is to establish a multi-modality cardiac image database including coronary angiography (CAG), optical coherence tomography (OCT), intravascular ultrasound (IVUS), computed tomography angiograms (CTA) and cardiac magnetic resonance imaging (CMR) for future studies. The main goal of this collaboration is to create a resource for advanced research on atherosclerosis through image analysis.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
240mo left

Started Aug 2025

Longer than P75 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress4%
Aug 2025Dec 2045

First Submitted

Initial submission to the registry

July 14, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 23, 2025

Completed
9 days until next milestone

Study Start

First participant enrolled

August 1, 2025

Completed
10.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2035

Expected
10 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2045

Last Updated

July 30, 2025

Status Verified

July 1, 2025

Enrollment Period

10.4 years

First QC Date

July 14, 2025

Last Update Submit

July 27, 2025

Conditions

Keywords

Computed Tomography AngiographyCoronary AngiographyIntravascular UltrasoundOptical Coherence TomographyCardiac Magnetic Resonance Imaging

Outcome Measures

Primary Outcomes (1)

  • MACE

    Major adverse cardiac events

    10 years

Study Arms (1)

Study cohort

Patients who underwent CAG or CTA during Aug 1st, 2025 and Dec 31st, 2035 at Zhongshan Hospital will be included in this registry. In addition, patients with CTA or at least one of OCT/IVUS/CMR between Jan 1st, 2012 and Jul 31st, 2025 will be retrospectively registered.

Other: Cardiac imaging

Interventions

Patients who underwent CTA or CAG, with or without other cardiac imaging modelities (OCT, IVUS, or CMR) will be enrolled in this registry.

Also known as: CAG/CTA/OCT/IVUS/CMR
Study cohort

Eligibility Criteria

Age14 Years - 99 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with potential cardiovascular disease(s) (CVD) or diagnosed with CVD who were referred to CTA and/or CAG at Zhongshan Hospital, Fudan university.

You may qualify if:

  • Patients with potential cardiovascular disease(s) (CVD) or diagnosed with CVD who were referred to CTA and/or CAG.
  • Optional cardiac imagings, namely OCT/IVUS/CMR were up to doctors in charge and not mandatory.

You may not qualify if:

  • Patient without any of the above mentioned cardiac imaging record.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

AtherosclerosisCardiovascular Diseases

Condition Hierarchy (Ancestors)

ArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Study Officials

  • Junbo Ge, MD, PhD

    Cardiovascular Department, Zhongshan Hospital, Fudan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Target Duration
10 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head of Department of Cardiology

Study Record Dates

First Submitted

July 14, 2025

First Posted

July 23, 2025

Study Start

August 1, 2025

Primary Completion (Estimated)

December 31, 2035

Study Completion (Estimated)

December 31, 2045

Last Updated

July 30, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

There is no plan to share IPD for this observational study.